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Organic 12: Polymers

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Total cards: 21•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

Define polymer.

Back (Answer)

Long chain molecule made from lots of smaller molecules joined together

#2
Front (Question)

Define monomer.

Back (Answer)

Small molecules that join together to make polymers

#3
Front (Question)

What is addition polymerisation?

Back (Answer)

The formation of long chain molecules from lots of small molecules joining together with no other products

#4
Front (Question)

What is condensation polymerisation?

Back (Answer)

The formation of long chain molecules from lots of small molecules joining together with another small molecule (e.g. water) produced as well

#5
Front (Question)

What monomers are used in addition polymerisation?

Back (Answer)

Alkenes (molecules with C=C bonds)

#6
Front (Question)

Are addition polymers biodegradable and why?

Back (Answer)

No, because there are no polar bonds in the main chain (all bonds are C-C)

#7
Front (Question)

Give two examples of addition polymers.

Back (Answer)

Poly(ethene) Poly(propene) Polychloroethene (PVC)

#8
Front (Question)

What monomers are used in condensation polymerisation?

Back (Answer)

Dicarboxylic acids + diols Dicarboxylic acids + diamines Amino acids

#9
Front (Question)

Give two examples of condensation polymers.

Back (Answer)

Polyesters (e.g. terylene) Polyamides (e.g. nylon, Kevlar) Polypeptides

#10
Front (Question)

Are condensation polymers biodegradable and why?

Back (Answer)

Yes, because there are polar C-N or C-O bonds in the main chain, so they can interact with water (i.e. be hydrolysed)

#11
Front (Question)

Why are addition polymers chemically inert?

Back (Answer)

Because all of the molecules are saturated (no double bonds)

#12
Front (Question)

What are the three ways of disposing of polymers?

Back (Answer)

Landfill Incineration Recycling

#13
Front (Question)

Describe each of the three ways of disposing of polymers giving advantages and disadvantages.

Back (Answer)

Landfill: Burying polymers in the ground Advantages: cheap, quick, simple Disadvantages: Stays in the ground for a long time (takes too long to biodegrade), plastic becomes brittle, could break up and be washed away into water sources Incineration: Burning polymers Advantages: No land pollution Heat generated can be used for electricity Disadvantages: Addition polymers produce CO (toxic) and CO2 (greenhouse gas) Condensation polymers can also produce toxic gases when incinerated Recycling: Collecting, washing, and sorting polymers, then cutting them into small parts to be reused Advantages: Not in landfill or being incinerated, so less land pollution and toxic gases Less energy needed to produce an item from recycled plastics than from new plastics Disadvantages: Logistics - relying on the public to recycle, can take a long time to collect it all

#14
Front (Question)

What type of plastic can’t be recycled?

Back (Answer)

Thermosetting plastics - they are heated once and they stay in that shape permanently

#15
Front (Question)

What do diols and dicarboxylic acids look like?

Back (Answer)

Diols have two hydroxyl (alcohol) groups Dicarboxylic acids have two COOH groups at either end

Card back image
#16
Front (Question)

Where do the condensation reactions happen between a dicarboxylic acid and a diol?

Back (Answer)

With the OH from the carboxylic acid and the H from the alcohol group

#17
Front (Question)

What type of polymer forms in a condensation reaction between a dicarboxylic acid and a diol?

Back (Answer)

Polyester (has repeated ester linkages)

Card back image
#18
Front (Question)

What type of polymer forms in a condensation reaction between a carboxylic acid and an amine?

Back (Answer)

Polyamide (has repeated amide linkages)

Card back image
#19
Front (Question)

What two monomers make up nylon 6,6?

Back (Answer)

1,6diaminohexane hexane-1,6dicarboxylic acid (polyamide linkages)

Card back image
#20
Front (Question)

What two monomers make up Kevlar?

Back (Answer)

Benzene-1,4-diamine Benzene-1,4-dicarboxylic acid (Polyamide linkages)

Card back image
#21
Front (Question)

Why is Kevlar so strong?

Back (Answer)

Due to the rigid chains and ability of the flat aromatic rings to pack together held by strong intermolecular forces